205444-34-4 Usage
Description
(S)-tert-butyl 2-(hydroxymethyl)-2,5-dihydro-1H-pyrrole-1-carboxylate is a chemical compound that belongs to the class of carboxylic acids and derivatives. It is a pyrrole derivative with a tert-butyl group attached to the nitrogen atom, and a hydroxymethyl group attached to the carbon atom. (S)-tert-butyl 2-(hydroxymethyl)-2,5-dihydro-1H-pyrrole-1-carboxylate is characterized by its potential applications in various fields due to its unique structural features and biological activities.
Uses
Used in Pharmaceutical Industry:
(S)-tert-butyl 2-(hydroxymethyl)-2,5-dihydro-1H-pyrrole-1-carboxylate is used as a building block for the synthesis of various pharmaceuticals. Its unique structure allows for the creation of a wide range of therapeutic compounds, making it a valuable asset in the development of new medications.
Used in Agrochemical Industry:
In the agrochemical industry, (S)-tert-butyl 2-(hydroxymethyl)-2,5-dihydro-1H-pyrrole-1-carboxylate is utilized as a key component in the synthesis of various agrochemicals. Its versatility in chemical reactions enables the production of compounds with specific pesticidal or herbicidal properties, contributing to the development of effective agricultural solutions.
Used in Organic Synthesis:
(S)-tert-butyl 2-(hydroxymethyl)-2,5-dihydro-1H-pyrrole-1-carboxylate is used as a chiral ligand in asymmetric synthesis reactions. Its presence in these reactions can lead to the formation of enantiomerically pure compounds, which are essential in various applications, including the production of pharmaceuticals with improved efficacy and reduced side effects.
Used in Biological Research:
Due to its potential biological activities, such as anti-inflammatory and anti-cancer properties, (S)-tert-butyl 2-(hydroxymethyl)-2,5-dihydro-1H-pyrrole-1-carboxylate is also used in biological research. Scientists are investigating its effects on various biological pathways to better understand its potential therapeutic applications and to develop new treatments for various diseases.
Check Digit Verification of cas no
The CAS Registry Mumber 205444-34-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,5,4,4 and 4 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 205444-34:
(8*2)+(7*0)+(6*5)+(5*4)+(4*4)+(3*4)+(2*3)+(1*4)=104
104 % 10 = 4
So 205444-34-4 is a valid CAS Registry Number.
205444-34-4Relevant articles and documents
Studies towards a total synthesis of kainic acid
Greenwood,Hitchcock,Parsons
, p. 3307 - 3314 (2007/10/03)
The preparation of the fused bicycle 14 is reported together with its photocyclisation to the dioxinone 2. Base induced fragmentation of the photoadduct 15 formed exclusively in the aforementioned photocylisation, followed by Wittig methylenation gave the kainoid derivative 18.
